# K190259: Vesta RF Cannula

- Pathway: 510(k) (Special)
- Applicant: Biomerics
- Decided: Feb 7, 2020 after 365 days
- Product code: GXI (Probe, Radiofrequency Lesion)
- Device class: 2
- Regulation: 21 CFR 882.4725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K972846 (1998). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K121773: Nimbus Electrosurgical Radiofrequency Multitined Expandable Electrode, Biomerics (2012) Summary page 4.

## Indications for use
The Vesta RF Cannula, in combination with an RF generator and probe, are intended for use in radiofrequency (RF) heat lesion procedures for relief of pain.

Source page: https://510kreport.com/device/K190259
Methodology: https://510kreport.com/methodology